Skip to content
Stop using now Food recall · FDA · Published May 23, 2018

New Seasons Mini Chocolate Croissant Recall: Undeclared Egg & Soy

New Seasons Market recalls Mini Chocolate Croissants due to undeclared egg and soy lecithin. Check your UPC and best-by date for details.

🇺🇸 FDA recall #F-1589-2018FoodNew Seasons Market ›
Take action

Contact the company

Recalling firmNew Seasons Market LLC1300 Se Stark St Ste 401 · Portland, OR 97214-2473
✎ GovInfoNow plain-language explainer

What happened, in plain English

New Seasons Market LLC is recalling Mini Chocolate Croissants, 8-Pack because the packaging fails to declare egg and soy lecithin as ingredients. This is a Class I recall, indicating a high hazard risk for individuals with severe allergies to these substances. The products were distributed in Oregon and Washington. Read more at govinfonow.com/recall/19097-new-seasons-mini-chocolate-croissant-recall-undeclared-egg-soy.

Source Summary by GovInfoNow · govinfonow.com/recall/19097-new-seasons-mini-chocolate-croissant-recall-undeclared-egg-soy · Updated October 11, 2026 · FDA enforcement record: FDA #F-1589-2018

Cite this page

“New Seasons Mini Chocolate Croissant Recall: Undeclared Egg & Soy.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/19097-new-seasons-mini-chocolate-croissant-recall-undeclared-egg-soy. Based on FDA recall #F-1589-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1589-2018%22&limit=1).

Why it’s dangerous

The product contains egg and soy lecithin, but these ingredients are not listed on the label. For people with severe allergies to eggs or soy, consuming this product could trigger a dangerous allergic reaction without their knowledge.

Who’s affected

Consumers who purchased the specific Mini Chocolate Croissants at New Seasons Market stores in Oregon or Washington are affected. Individuals with egg or soy allergies are at the highest risk of serious allergic reaction.

How to tell if you have this one

Look for Mini Chocolate Croissants, 8-Pack in a clear plastic clam-shell container with a net weight of 7.6 oz. The UPC is 8 04600 10905 1. Check the package for a 'Best by' date of up to and including 5/27/2018.

  • Brand
    New Seasons Market
  • Category
    Food
FDA recall event · 6 products

All 6 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Status
    Terminated
  • Distribution
    Distributed in OR and WA
Recall numberProduct, codes & lotsQuantityClass
F-1584-2018Honey Oat Bran Muffin, 4-pack, packaged in a clear clamshell container, net wt. 13.6 oz., UPC 8 40600 10954 9; Best by up to and includes 5/27/2018199 packages (4 pieces per package)Class III
F-1585-2018Meyer Lemon Chia Muffin, 4-pack, packaged in a clear clamshell container, net wt. 13.6 oz., UPC 8 40600 10953 2; Best by up to and includes 5/27/2018241 packages (4 pieces per package)Class II
F-1586-2018Blueberry Buckwheat Muffin, 4-pack, packaged in a clear clamshell container, net wt. 13.6 oz., UPC 8 40600 10952 5; Best by up to and includes 5/27/2018233 packages (4 pieces per package)Class II
F-1587-2018Vegan Chocolate Almond Muffin, 4-pack, packaged in a clear clamshell container, net wt. 13.6 oz., UPC 8 40600 10955 6; Best by up to and includes 5/27/2018156 packages (4 pieces per package)Class III
F-1588-2018Mini Butter Croissants, 8-Pack, packaged in a clear plastic clam-shell container, net wt. 6 oz., UPC 8 40600 10904 4; Best by up to and includes 5/27/2018314 packages (8 pieces per package)Class I
F-1589-2018Mini Chocolate Croissants, 8-Pack, packaged in a clear plastic clam-shell container, net wt. 7.6 oz., UPC 8 04600 10905 1; Best by up to and includes 5/27/2018299 packages (8 pieces per package)Class I
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the Mini Chocolate Croissants if you have egg or soy allergies.

  2. Check your package details

    Verify that your package matches the UPC 8 04600 10905 1 and has a best-by date on or before May 27, 2018.

  3. Discard or return the item

    The record does not specify a specific remedy such as a refund or replacement; consumers should dispose of the product to avoid accidental consumption.

Where it went and when

Where it was distributed

Distributed in Oregon and Washington.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Distributed in OR and WA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Oregon, Washington.

Recall timeline

FDA terminated this recall 37 days after the firm started it.

1. Firm started the recall: May 23, 201812. FDA classified it Class I: Jun 22, 201823. FDA terminated the recall: Jun 29, 201834. Published in FDA’s Enforcement Report: Jul 4, 201842018
  1. Firm started the recall
  2. FDA classified it Class I
  3. FDA terminated the recall
  4. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

Similar recalls

Latest food recalls

Keep exploring

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-1589-2018 (May 23, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1589-2018 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA